5-Bromo-1-indanone → HCID 24987025, compound

HRID 2251645Notes

Reaction equation

HRID 2251645 reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[C:7](=[O:11])[CH2:6][CH2:5]2.[C:12]([C:14]1[CH:15]=[C:16](B(O)O)[CH:17]=[CH:18][CH:19]=1)#[N:13]>>[O:11]=[C:7]1[C:8]2[C:4](=[CH:3][C:2]([C:18]3[CH:19]=[C:14]([CH:15]=[CH:16][CH:17]=3)[C:12]#[N:13])=[CH:10][CH:9]=2)[CH2:5][CH2:6]1

Participants

3

Reactant 2

HCID 5206955-Bromo-1-indanoneHCID 27343253-Cyanophenylboronic acid

Product 1

HCID 24987025HCID 24987025, compound

Procedure

The title compound was prepared from 5-bromo-1-indanone and 3-cyanophenyl boronic acid according to the coupling procedure as described in example 6. MS m/z 234; HRMS: calcd for C16H11NO+H+, 234.09134; found (ESI, [M+H]+), 234.0905;

Sources & evidence

ORD record
ord-ebab064ac26343dea8ad4fc90b76dc04
Source dataset
uspto-grants-2008_01
Patent number
US07319152B2

Reaction notes

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